Jillian R. Ozmore

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

Santhosh Girirajan, Jill A. Rosenfeld, Gregory M. Cooper et al. · Nature Genetics · 2010 · 674 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP

Anke Van Dijck, Anneke T. Vulto‐van Silfhout, Elisa Cappuyns et al. · Biological Psychiatry · 2018 · 182 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes

Cynthia J. Curry, Jill A. Rosenfeld, Erica T. Grant et al. · American Journal of Medical Genetics Part A · 2013 · 105 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Initial Transcribed Sequence Mutations Specifically Affect Promoter Escape Properties

Lilian M. Hsu, Ingrid M. Cobb, Jillian R. Ozmore et al. · Biochemistry · 2006 · 56 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors

John Herriges, Sara Brown, Maria Longhurst et al. · European Journal of Medical Genetics · 2018 · 22 citations

Medicine, Molecular Genetics, Oncology +10